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tert-butyl azidoformate

Product Name
tert-butyl azidoformate
CAS No.
1070-19-5
Chemical Name
tert-butyl azidoformate
Synonyms
t-Butyl Azidoformate;tert-butyl azidoformate;Azacitidine Impurity 52;ert-butylN-diazocarbamate;Azido tert-butoxymethanone;(tert-Butoxycarbonyl) azide;tert-butyl N-diazocarbamate;N-(tert-butyloxycarbonyl) azide;Azidoformic acid tert-butyl ester;Azidocarbonic acid tert-butyl ester
CBNumber
CB5892220
Molecular Formula
C5H9N3O2
Formula Weight
143.14386
MOL File
1070-19-5.mol
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tert-butyl azidoformate Property

Boiling point:
261.22°C (rough estimate)
Density 
1.3172 (rough estimate)
refractive index 
1.6190 (estimate)
EPA Substance Registry System
Carbonazidic acid, 1,1-dimethylethyl ester (1070-19-5)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM1015342
Product name
TERT-BUTYL AZIDOFORMATE
Purity
95.00%
Packaging
5MG
Price
$499.65
Updated
2021/12/16
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tert-butyl azidoformate Chemical Properties,Usage,Production

Uses

t-Butyl azidoformate is a convenient reagent for the acylation of amines, hydrazines, and similar compounds.

Preparation

tert-Butyl chloroformate was prepared in solution as follows. Dry phosgene was introduced into a solution of 18 g (0.24 mol) of tert-butyl alcohol in 500 ml of anhydrous ether until about 52 g (0.5 mol) had been absorbed and the mixture was cooled in a Dry Ice-acetone bath. Then a solution of 20 g (0.28 mol) of pyridine in 200 ml of anhydrous ether was added dropwise with vigorous stirring. The reaction mixture was stored overnight in a Dry Ice box. The precipitated pyridine hydrochloride was filtered and the volume of the filtrate was reduced to -70 ml at reduced pressure with cooling in an icewater bath.This cold solution of tert-butyl chloroformate was added over 30 min to a vigorously stirred solution of 31.6 g (0.2 mol) of tetramethylguanidinium azide in 200 ml of chloroform; the temperature was kept at 0°C throughout the addition. The bath was removed and the reaction mixture stirred for an additional hour and then poured into 500 nil of ice water containing -2 ml of acetic acid. Extraction with two 60-ml portions of ether followed by careful evaporation of the dried (magnesium sulfate) organic phase gave tert-butyl azidoformate as a pale amber liquid in quantitative yield.
The Direct Preparation of tert-Butyl Azidoformate

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 955, 1959 DOI: 10.1021/ja01513a049
Tetrahedron Letters, 25, p. 3701, 1984 DOI: 10.1016/0040-4039(84)80109-4

Safety Profile

An unstable shockand heat-sensitive explosive. It may explode above 100°C and iptes at 143°C. When heated to decomposition it emits toxic fumes of NOx. See also AZIDES.

tert-butyl azidoformate Preparation Products And Raw materials

Raw materials

Preparation Products

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tert-butyl azidoformate Suppliers

Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71

1070-19-5, tert-butyl azidoformateRelated Search:


  • tert-butyl azidoformate
  • (tert-Butoxycarbonyl) azide
  • Azido tert-butoxymethanone
  • Azidocarbonic acid tert-butyl ester
  • Azidoformic acid tert-butyl ester
  • t-Butyl Azidoformate
  • N-(tert-butyloxycarbonyl) azide
  • tert-butyl N-diazocarbamate
  • ert-butylN-diazocarbamate
  • Azacitidine Impurity 52
  • 1070-19-5